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93030006: Congenital absence of spleen (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
153877013 Congenital absence of spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
153878015 Congenital asplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836678011 Congenital absence of spleen (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
153877013 Congenital absence of spleen en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
153877013 Congenital absence of spleen en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
153878015 Congenital asplenia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
153878015 Congenital asplenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836678011 Congenital absence of spleen (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836678011 Congenital absence of spleen (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235779019 Splenic agenesis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1235779019 Splenic agenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235780016 Splenic aplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4706211000241119 absence congénitale de la rate fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4706211000241119 absence congénitale de la rate fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of spleen Is a Congenital anomaly of spleen true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of spleen Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Finding site Splenic structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of spleen Finding site Splenic structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of spleen Is a Aplasia of spleen (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Is a Congenital absence false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital absence of spleen Is a Asplenia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence of spleen Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Associated morphology Agenesis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Finding site Entire spleen false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of spleen Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Functional asplenia Is a False Congenital absence of spleen Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral right-sidedness sequence Is a False Congenital absence of spleen Inferred relationship Existential restriction modifier (core metadata concept)
Familial isolated congenital asplenia (disorder) Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier (core metadata concept)
Agenesis of spleen Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital diaphragmatic hernia, short bowel, and asplenia. Dysmorphic facial features include long forehead, hypertelorism, upturned nares, and small mandible. Atresia of the duodenum has also been reported. Is a True Congenital absence of spleen Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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